Canonical Allele Identifier: PA2826942295
Gene: CHRND HGNC NCBI

Linked Data

ClinVar Variation Id: 1387239
ClinVar RCV Id: RCV001881846
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001298124.1:p.Arg218Lys
CA66957565
NM_001311195.2:c.653G>A